Evaluation of the Efficacy of Azithromycin to Prevent Bronchiolitis Obliterans Syndrome After Allogeneic Hematopoietic Stem Cell Transplantation
试验速览
- 阶段
- 3 期
- 入组人数
- 480
- 试验地点
- 1
- 主要终点
- Airflow decline (AFD)-free survival
研究概览
简要总结
The occurrence of bronchiolitis obliterans syndrome (SBO) after allogeneic hematopoietic stem cell transplantation (HSCT) is considered to be a chronic pulmonary graft versus host disease (GVHD) that is associated with significant mortality and morbidity. The reported incidence of SBO varies from 6 to 26% of allogeneic HSC recipients and is usually diagnosed within 2 years after transplantation. The diagnosis of SBO relies on the occurrence of a new airflow obstruction identified during pulmonary function testing, and the definition differs between studies. Currently, no curative immunosuppressive treatment is available, and recent data suggest that the use of these treatments, especially corticosteroids, should be limited because of their toxicity. The impairment of lung function parameters is likely caused by fibrous small airway lesions. Few data on the pathogenesis of SBO after allogeneic HSCT are available. Several hypotheses are based on the occurrence of SBO during chronic graft rejection after lung transplantation, which shares many clinical and histopathological similarities with SBO after allogeneic HSCT. One hypothesis is that the first step leading to SBO is lung epithelium injury. SBO is then identified as an alloimmune reaction with only one clearly identified risk factor: extrathoracic chronic GVHD. Due to their anti-inflammatory and immunomodulatory properties, recent data suggest that low-dose macrolides may be effective at preventing SBO after lung transplants. This well-tolerated treatment may be useful for preventing SBO after allogeneic HSCT.
The objective of this Phase 3 multicentre randomized, double-blinded, clinical trial is to evaluate the efficacy of azithromycin in preventing BO syndrome after allogeneic HSCT in patients with malignant hematological diseases.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Prevention
- 盲法
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 16 Years 至 —(Child, Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients> 16 years old
- •Experimenting an allogeneic HSCT for a hematologic malignancy
- •Pre-transplantation Pulmonary Function Testing
- •With written informed consent
排除标准
- •Allergy or Intolerance to azithromycin, macrolides or ketolide or excipient
- •Prolonged corrected QT (QTc) interval (>450 msec)
- •Taking medications that prolong the QTc interval (Cisapride, ergotamine, dyhydroergotamine)
- •Taking ergotamine and dyhydroergotamine due to the risk of ergotism
- •Family history of a prolonged QTc interval.
- •History of congestive heart failure
- •Taking colchicine Severe liver insufficiency • History of infection due to atypical mycobacteria
研究组 & 干预措施
Azithromycine
250 mg x 3/week during a meal for a period of 2 years
干预措施: Azithromycin (Drug)
Placebo
250 mg x 3/week during a meal for a period of 2 years.
干预措施: Placebo (Drug)
结局指标
主要结局
Airflow decline (AFD)-free survival
时间窗: 2 year after allogeneic HSCT
Defined on the criteria from Chien JW et al (Am J Resp Crit Care Med 2003;168:208-14) by an annualized decline of percent predicted forced expiratory volume in 1 second (FEV1) of more than 5%
次要结局
- Overall survival(within 2 years of inclusion)
- Occurrence of late-onset pulmonary non-infectious complications (=bronchiolitis obliterans syndrome, SBO)(within 2 years after inclusion)
- Occurrence of acute and chronic extra-thoracic graft versus host disease (GVHD)(within 2 years after inclusion)
- Cumulative incidence of hematological relapse(within the 2 years after inclusion)
- Quality of life(within 2 years after inclusion)
- Cumulative dose of steroids treatment(within the 2 years after inclusion)
- Variation of pulmonary function testing parameters(within 2 years after inclusion)
- Tolerance(within 2 years of inclusion)
